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Register to vote Register by 18 June to vote in the General Election on 4 July.
How to apply for marketing authorisation via this new procedure.
An explanation of how UKHSA processes your personal data when you apply to access it for secondary purposes
How to use an ethnographic study to evaluate your digital health product.
Cyber Defence and Risk (CyDR) defence industry ICT accreditation and risk balance case (RBC) processes.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
How to begin with evaluating a digital health product, including when to evaluate, budgeting and getting support.
How GBN’s technology selection process for Small Modular Reactors (SMRs) will work.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Design, build and operate APIs in a consistent way
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
The 12-stage process on how a marine plan is made from selection to implementation and monitoring and how you can get involved.
Using an ecological momentary assessment to evaluate your digital health product.
Find out about how we manage unacceptable behaviour consistently and fairly.
Emerging techniques on how to prevent or minimise the environmental impacts of industrial hydrogen production from methane or refinery fuel gas with carbon capture for storage.
Improving victims engagement in the parole process
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Submission dates and how the submissions using the EC decision reliance procedure work.
The Local Plan examination process and the role the Planning Inspectorate plays.
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